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I型干扰素产生的“无 Toll 样受体”途径

"Toll-free" pathways for production of type I interferons.

作者信息

Wang Ling, Ning Shunbin

机构信息

Department of Internal Medicine, Quillen College of Medicine, East Tennessee State University, Johnson City, TN 37614, USA.

Center of Excellence for Inflammation, Infectious Diseases and Immunity, Quillen College of Medicine, East Tennessee State University, Johnson City, TN 37614, USA.

出版信息

AIMS Allergy Immunol. 2017;1(3):143-163. doi: 10.3934/Allergy.2017.3.143. Epub 2017 Nov 6.

Abstract

Pathogen-associated molecular patterns (PAMPs) and damage-associated molecular patterns (DAMPs) are recognized by different cellular pathogen recognition receptors (PRRs), which are expressed on cell membrane or in the cytoplasm of cells of the innate immune system. Nucleic acids derived from pathogens or from certain cellular conditions represent a large category of PAMPs/DAMPs that trigger production of type I interferons (IFN-I) in addition to pro-inflammatory cytokines, by specifically binding to intracellular Toll-like receptors or cytosolic receptors. These cytosolic receptors, which are not related to TLRs and we call them "Toll-free" receptors, include the RNA-sensing RIG-I like receptors (RLRs), the DNA-sensing HIN200 family, and cGAS, amongst others. Viruses have evolved myriad strategies to evoke both host cellular and viral factors to evade IFN-I-mediated innate immune responses, to facilitate their infection, replication, and establishment of latency. This review outlines these "Toll-free" innate immune pathways and recent updates on their regulation, with focus on cellular and viral factors with enzyme activities.

摘要

病原体相关分子模式(PAMPs)和损伤相关分子模式(DAMPs)由不同的细胞病原体识别受体(PRRs)识别,这些受体表达于固有免疫系统细胞的细胞膜或细胞质中。来自病原体或某些细胞状况的核酸代表了一大类PAMPs/DAMPs,它们通过与细胞内Toll样受体或胞质受体特异性结合,除了促炎细胞因子外,还触发I型干扰素(IFN-I)的产生。这些与Toll样受体无关的胞质受体,我们称之为“无Toll样受体”受体,包括RNA传感RIG-I样受体(RLRs)、DNA传感HIN200家族和cGAS等。病毒已经进化出无数策略来激活宿主细胞和病毒因子,以逃避IFN-I介导的固有免疫反应,促进其感染、复制和潜伏的建立。本综述概述了这些“无Toll样受体”的固有免疫途径及其调控的最新进展,重点关注具有酶活性的细胞和病毒因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e19/5710802/13edf2f3e6c7/nihms918441f1.jpg

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